Antimicrobial Susceptibility and Genetic Epidemiology of Extended-Spectrum β-Lactamase-Positive Enterobacterales Clinical Isolates in Central Poland.
Małgorzata BrauncajsFilip BielecAnna MaciejaPiotr MachnickiDorota Pastuszak-LewandoskaPublished in: International journal of molecular sciences (2024)
The extended-spectrum β-lactamases (ESβLs) are bacterial enzymes capable of hydrolyzing penicillins, cephalosporins, and aztreonam. The prevalence of ESβL is increasing among clinically significant microorganisms worldwide, drastically reducing the therapeutic management of infectious diseases. The study aimed to determine the drug susceptibility of ESβL-positive clinical isolates acquired from patients hospitalized in Lodz, central Poland, and analyze the prevalence of specific genes, determining acquired resistance in these bacteria. The samples of ESβL-positive clinical isolates were gathered in 2022 from medical microbiological laboratories in the city of Lodz, central Poland. The strains were subjected to biochemical identification and antimicrobial susceptibility testing following EUCAST guidelines. The presence of studied genes (bla CTX-M , bla SHV , bla TEM , bla PER , bla VEB ) was confirmed by PCR. Over 50% of studied isolates were resistant to gentamicin, cefepime, ceftazidime and ciprofloxacin. The most common ESβL gene was bla CTX-M . In most isolates, the resistance genes occurred simultaneously. The bla PER was not detected in any of the tested strains. ESβL-producing strains are largely susceptible to the currently available antibiotics. The observation of the coexistence of different genes in most clinical isolates is alarming.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- genome wide
- multidrug resistant
- bioinformatics analysis
- genome wide identification
- infectious diseases
- end stage renal disease
- risk factors
- dna methylation
- genome wide analysis
- chronic kidney disease
- gram negative
- copy number
- pseudomonas aeruginosa
- ejection fraction
- emergency department
- prognostic factors
- gene expression
- peritoneal dialysis
- patient reported outcomes
- adverse drug
- cystic fibrosis